Robust synthesis of enantiopure cyclohexenyl analogues of 2/3-deoxyribose sugars as carbocyclic nucleoside precursors

TitleRobust synthesis of enantiopure cyclohexenyl analogues of 2/3-deoxyribose sugars as carbocyclic nucleoside precursors
Publication TypeJournal Article
Year of Publication2011
AuthorsVarada, M, Kotikam, V, Kumar, VA
JournalTetrahedron
Volume67
Issue32
Pagination5744-5749
Date PublishedAUG
ISSN0040-4020
KeywordsCarbocyclic mimics of 2-deoxy-D-ribose and 3-deoxy-D-ribose Enzymatic resolution, CeNA, DA reaction
Abstract

An expedient synthesis of 2-deoxy (10) and 3-deoxy (11) cyclohexenyl analogues of 2-deoxy and 3-deoxy-D-ribose sugar from commercially available starting materials is reported. Highly efficient enzymatic resolution of the key compound 10 is described using lipase under hydrolytic conditions. The robust methodology applied here will be useful to synthesize cyclohexenyl nucleosides, which possess potent antiviral activity and are capable of gene silencing via RNAi or antisense applications. (C) 2011 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tet.2011.06.003
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)3.025
Divison category: 
Organic Chemistry